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Andrology

Genetic Test
Samples Required
EDTA

Kallmann Syndrome (microdeletion Gene Kal1)

SKU MBG-A1114
Categories , , ,
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Description

Kallmann syndrome (KS) is a developmental genetic disorder characterized by the association of congenital hypogonadotropic hypogonadism (CHH) due to gonadotropin-releasing hormone (GnRH) deficiency, and anosmia or hyposmia (with hypoplasia or aplasia of the olfactory bulbs).

External Information

Click here for more information about the Kallmann Syndrome (microdeletion Gene Kal1) genetic test.

Additional information

Samples

EDTA, LA, VC
Method of testing

A.CGH
Turnaround Time (TAT) 3-7 days
Number of Genes

1
Genes / Chromosomes / SNPs

KAL1 (del Xp22.31)
External Information Click here for more information about the Kallmann Syndrome (microdeletion Gene Kal1) genetic test.

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